Peter McColgan
Peter McColgan
University College London
Email verificata su qub.ac.uk
Titolo
Citata da
Citata da
Anno
Huntington's disease: a clinical review
P McColgan, SJ Tabrizi
European journal of neurology 25 (1), 24-34, 2018
2482018
C9orf72 expansions are the most common genetic cause of Huntington disease phenocopies
DJH Moss, M Poulter, J Beck, J Hehir, JM Polke, T Campbell, G Adamson, ...
Neurology 82 (4), 292-299, 2014
1722014
Towards the identification of blood biomarkers for acute stroke in humans: a comprehensive systematic review
N Hasan, P McColgan, P Bentley, RJ Edwards, P Sharma
British journal of clinical pharmacology 74 (2), 230-240, 2012
1272012
The Addenbrooke's Cognitive Examination for the differential diagnosis and longitudinal assessment of patients with parkinsonian disorders
T Rittman, BC Ghosh, P McColgan, DP Breen, J Evans, CH Williams-Gray, ...
Journal of Neurology, Neurosurgery & Psychiatry 84 (5), 544-551, 2013
842013
Large-scale DCMs for resting-state fMRI
A Razi, ML Seghier, Y Zhou, P McColgan, P Zeidman, HJ Park, O Sporns, ...
Network Neuroscience 1 (3), 222-241, 2017
622017
Selective vulnerability of Rich Club brain regions is an organizational principle of structural connectivity loss in Huntington’s disease
P McColgan, KK Seunarine, A Razi, JH Cole, S Gregory, A Durr, ...
Brain 138 (11), 3327-3344, 2015
592015
The genetics of sporadic ruptured and unruptured intracranial aneurysms: a genetic meta-analysis of 8 genes and 13 polymorphisms in approximately 20,000 individuals
P McColgan, KZ Thant, P Sharma
Journal of neurosurgery 112 (4), 714-721, 2010
572010
Polymorphisms of matrix metalloproteinases 1, 2, 3 and 9 and susceptibility to lung, breast and colorectal cancer in over 30,000 subjects
P McColgan, P Sharma
International journal of cancer 125 (6), 1473-1478, 2009
562009
Stem cell tracking in human trials: a meta-regression
P McColgan, P Sharma, P Bentley
Stem Cell Reviews and Reports 7 (4), 1031-1040, 2011
412011
Addenbrooke's Cognitive Examination‐Revised for mild cognitive impairment in Parkinson's disease
P McColgan, JR Evans, DP Breen, SL Mason, RA Barker, ...
Movement Disorders 27 (9), 1173-1177, 2012
402012
Educational interventions in neurology: a comprehensive systematic review
P McColgan, PP McKeown, C Selai, R Doherty‐Allan, MO McCarron
European Journal of Neurology 20 (7), 1006-1016, 2013
362013
Cerebrospinal fluid total tau concentration predicts clinical phenotype in Huntington's disease
FB Rodrigues, L Byrne, P McColgan, N Robertson, SJ Tabrizi, BR Leavitt, ...
Journal of neurochemistry 139 (1), 22-25, 2016
352016
The genetics of abdominal aortic aneurysms: a comprehensive meta-analysis involving eight candidate genes in over 16,700 patients.
P McColgan, GE Peck, RM Greenhalgh, P Sharma
International surgery 94 (4), 350-358, 2009
352009
Brain regions showing white matter loss in Huntington’s disease are enriched for synaptic and metabolic genes
P McColgan, S Gregory, KK Seunarine, A Razi, M Papoutsi, E Johnson, ...
Biological psychiatry 83 (5), 456-465, 2018
342018
Cerebrospinal fluid inflammatory biomarkers reflect clinical severity in Huntington’s disease
FB Rodrigues, LM Byrne, P McColgan, N Robertson, SJ Tabrizi, ...
PloS one 11 (9), e0163479, 2016
302016
Basal ganglia‐cortical structural connectivity in Huntington's disease
MJU Novak, KK Seunarine, CR Gibbard, P McColgan, B Draganski, ...
Human brain mapping 36 (5), 1728-1740, 2015
302015
Can neuroimaging predict dementia in Parkinson’s disease?
JH Lanskey, P McColgan, AE Schrag, J Acosta-Cabronero, G Rees, ...
Brain 141 (9), 2545-2560, 2018
242018
Evaluation of the clinical utility of a carotid bruit
P McColgan, P Bentley, M McCarron, P Sharma
QJM: An International Journal of Medicine 105 (12), 1171-1177, 2012
222012
Topological length of white matter connections predicts their rate of atrophy in premanifest Huntington’s disease
P McColgan, KK Seunarine, S Gregory, A Razi, M Papoutsi, JD Long, ...
JCI insight 2 (8), 2017
212017
The genetics of carotid dissection: meta-analysis of a MTHFR/C677T common molecular variant
P McColgan, P Sharma
Cerebrovascular Diseases 25 (6), 561-565, 2008
202008
Il sistema al momento non pu eseguire l'operazione. Riprova pi tardi.
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